HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375702Erstellt: 25. Oktober 2026
Rofecoxib → (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol
https://huagongshe.com/reaction/1375702
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Rofecoxib | HCID 5090 | — |
| Edukt | Diisobutylaluminum hydride | HCID 14487 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol | HCID 57434773 | 98,7% |
Reaktionsschritte
To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2H), 7.36 (d, 2H), 7.16–7.05 (m, 5H), 4.66 (d, 2H), 4.63 (d, 2H), 4.19 (t, 1H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07169809B2 |
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| Quelldatensatz | uspto-grants-2007_01 |
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| ORD ID | ord-5edd1a315fdf4ebbb46c36c2676df4c7 |
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| Quellennotiz | uspto-grants-2007_01 |
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